Wireless chronic implant

ABSTRACT

A minimally invasive system for a wireless circulatory support pump that utilizes a low profile catheter-based techniques and provides temporary and chronic circulatory support depending on the needs of the subject. The system includes a wireless circulatory assist pump, a deployment catheter, and a retrieval catheter for inserting and removing the wireless circulatory assist pump from a subject. The wireless circulatory support pump is relatively easy to place, has high flow rates, and provide improvements in the subject&#39;s renal function.

TECHNICAL FIELD

The application relates generally to medical devices, and more particularly to a system, apparatus, and associated methods for assisting a subject's heart to pump blood (e.g., a circulatory assist pump).

BACKGROUND

U.S. Pat. No. 8,617,239 to Reitan (Dec. 13, 2013), the contents of which are incorporated herein by this reference, relates to a catheter pump to be positioned in the ascending aorta near the aortic valve of a human being, comprising an elongated sleeve with a drive cable extending through the sleeve and connectable at its end to an external drive source and a drive rotor near the distal end of the drive cable mounted on a drive shaft being connected with the drive cable. The drive rotor consists of a propeller enclosed in a cage and the propeller and the cage are foldable from an insertion position close to the drive shaft to an expanded working position, which are characterized by means for anchoring the drive rotor in the ascending aorta near the aortic valve after insertion. Also described is a method to position the pump of a catheter pump in the ascending aorta just above the aortic valve.

U.S. Pat. No. 8,617,239 to Reitan builds upon an earlier patent of Reitan, i.e., U.S. Pat. No. 5,749,855 to Reitan (May 12, 1998), the contents of which are also incorporated herein by this reference, which relates to a drive cable, with one end of the drive cable being connectable to a drive source and a collapsible drive propeller at the other end of the drive cable. The collapsible drive propeller is adjustable between a closed configuration in which the collapsible drive propeller is collapsed on the drive cable and an open configuration in which the collapsible drive propeller is expanded so as to be operative as an impeller. A sleeve extends between one side of the collapsible drive propeller and the other side of the collapsible drive propeller with the sleeve being movable between configurations in which the collapsible drive propeller is in the open and closed configuration. A lattice cage is arranged surrounding the propeller and is folded out at the same time as the propeller. As described by U.S. Pat. No. 8,617,239 to Reitan, while the device of U.S. Pat. No. 5,749,855 operates very well in many circumstances, there is still room for improvement.

An even earlier blood pumping catheter is described in U.S. Pat. No. 4,753,221 to Kensey et al. (Jun. 28, 1988), the contents of which are incorporated herein by this reference. Kensey et al. relates to an elongated catheter for pumping blood through at least a portion of a subject's vascular system. The catheter is of a sufficiently small diameter and flexibility to enable it to be passed through the vascular system so that the distal end portion of the catheter is located within or adjacent the subject's heart. A rotatable pump is located at the distal end of the catheter and is rotated by drive means in the catheter. The distal end portion of the catheter includes an inlet for blood to flow therein and an outlet for blood to flow therefrom. The catheter is arranged so that blood is pumped by the catheter's pump through the heart and into the vascular system without requiring any pumping action of the heart.

Other catheter pumps are known from US 2008/0132748 A1, US 2008/0114339 A1, and WO03/103745A2, the contents of each of which are incorporated herein by this reference.

BRIEF SUMMARY

Described, among other things herein, is a minimally invasive system for a wireless circulatory assist pump. The wireless circulatory assist pump uses a low profile, catheter-based technique and can be used to provide temporary and/or chronic circulatory support depending on the needs of the subject (e.g., a mammal, such as a human). The system may also include a deployment catheter, and a retrieval catheter for inserting and removing the wireless circulatory assist pump from a subject.

In certain embodiments, the described device may include a battery (or electrical storage device) powered circulatory assist pump (or pumps) positioned within an aortic stent which may be wirelessly charged with an abdominal belt.

The described wireless circulatory assist pumps are relatively easy to place, have higher flow rates than existing systems, and provide improvements in a subject's renal function. The chronic circulatory assist pump (which is removable) is placed within an aortic stent that is preferably wirelessly powered. The impeller is shaped and designed to maximize safety and blood flow and to reduce the risk of hemolysis.

In use, the catheter may be introduced “percutaneously” into the lower aorta via, e.g., the normal “Seldinger technique” in the groin (a small incision into the femoral artery) and fed up to the aorta to the desired position (e.g., the descending aorta). The pump may be inserted in the groin area and introduced into the femoral artery (e.g., to just above the renal arteries in the descending aorta) with the help of a small surgical insertion and insertion sheath. The pump is thereafter fed up into the desired position in the lower aorta.

Alternatively, the pump may be placed via axillary entry in the neck or chest of the subject. See, e.g., K M. Doersch, “Temporary Left Ventricular Assist Device Through an Axillary Access is a Promising Approach to Improve Outcomes in Refractory Cardiogenic Shock Patients,” ASAIO J. 2015 May-Jun; 61(3): 253-258; doi: 10.1097/MAT.0000000000000222, the contents of which are incorporated herein by this reference, which describes implantation of a temporary left ventricular assist device (“LVAD”) through an axillary approach as a way to provide adequate circulation to the subject, avoid multiple chest entries and infection risks.

When the catheter is disconnected from the stent after placement in the aorta, the stent can be switched to wireless power. The wireless electromagnetic power communicates directly with, e.g., iron filled (+) and (−) polarized tips of impeller blades. The pump may be combined with a removable wireless powered pulsatile mesh stent, which is placed above the catheter higher in the aorta. QUT repeater technology may be included for enhanced wireless power. “Wireless system to power heart pumps could save lives currently lost to infection” (May 15, 2017, Queensland University of Technology), phys.org/news/2017-05-wireless-power-heart-lost-infection.html, the contents of which are incorporated herein by this reference.

In some embodiments, a battery and motor are utilized to drive the pump. An external belt may be provided that wirelessly charges the battery. The external belt or vest (electric powered coil inside that extends along the length of the belt such that the coil surrounds the subject's abdomen when worn) and appropriate circuitry, which belt or vest provides an electromagnetic field. For example, a transmitting coil associated with the belt or vest transmits AC energy, which is received by a receiving coil associated with the wireless pump, which DC energy can be used to power a motor (e.g., pump) and/or a battery.

Also described are methods for providing circulatory assist to a subject in need thereof, the method comprising: using the described systems to provide circulatory assist to the subject. Such methods include methods where a “puckless” TET is positioned within a subject's vasculature such as within the aorta, including the descending aorta.

Further described is a system that may be used to provide circulatory assist support by maximizing cardio and renal function recovery, while at the same time minimizing risk of thrombosis, stroke, hemolysis, mechanical breakdown, infection, and heart valve damage. Further, because the impeller is positioned relatively far from the heart (e.g., just above the renal arteries in the aorta, see Int. J. Card. 2018; 275 (2019)53-58), the natural pulsatility of a heart beat is maintained. The impeller simply works in cooperation and harmony with the pulse waves. In contrast, prior art placement within or near the heart interferes with natural pulsatility. Preferably, flow and energy use are optimized via timing of pulsations and impeller turn speeds with natural heart pulsatile flow.

The system or “loop” may be automatically read and adjusted to maximize power usage, battery life, long term durability, flow, and patient blood pressure(s) that self-adjusts automatically in response to changing conditions of the patient such as sleep and exercise.

In certain embodiments, sensors are used with the system, e.g., to monitor hemolysis and/or impeller speed, and the pulsations of cuffs are adjusted as desired to balance a minimization of hemolysis with a maximization of flow utilizing the system.

In certain embodiments, a pulsating stent graft in the patient's upper aorta and an impeller turning circulatory assist pump placed in a bare aortic stent in the patient's lower aorta may be used in combination, with timing optimized. For instance, appropriately placed sensors may be used to optimize the timing of pulsations of the upper aortic stent graft and the revolutions per minute of a lower bare aortic stent impeller circulatory assist pump.

In order to avoid thrombo-embolismic complications, the circulatory assist pump or parts thereof can be, e.g., heparinized.

The actuation cable can be in the form of a compact cable that runs through the tubular elongated casing of the catheter. The actuation cable has such a construction that the impeller folds outwardly with forward movement of the actuation cable by the physician.

The tubular elongated casing can be surrounded by a sleeve or a tube of an elastic material such as rubber or similar.

In its extended condition, the impeller preferably has a working diameter about 23 mm for an adult human.

In practice, the described system may be used to not only sustain a (e.g., congestive heart failure) patient's life, but also may be used to provide mechanical circulatory assistance for, e.g., up to 36 months, during the course of heart rehabilitation/regeneration treatment.

The described system offers advantages over existing heart assist devices in that it need not cross the aortic valve, and location positioning of the device is not as strict as with existing devices, meaning there is less need to reposition the device. Furthermore, the system maintains arterial pulsatility, does not require a high pump speed (e.g., 7,500 vs. 33,000 rpm), reduces hemolysis, and reduces acute kidney injury.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 depicts a front view of an impeller in a deployed (or extended) position, in accordance with embodiments of the disclosure.

FIG. 2 depicts a top view of the impeller of FIG. 1 in a deployed (or extended) position, in accordance with embodiments of the disclosure.

FIG. 3 depicts a side view of the impeller of FIG. 1 in a stowed (or retracted) position, in accordance with embodiments of the disclosure.

FIG. 4 depicts a cross-sectional top view of the impeller of FIG. 1 in a deployed (or extended) position, in accordance with embodiments of the disclosure.

FIGS. 5 and 6 depict perspective views of blades of the impeller of FIG. 1 , in accordance with embodiments of the disclosure.

FIG. 7 is a picture of a device as described herein connected to a drive axis placed within a pig.

FIG. 8 shows an overall schematic of a system according to the disclosure (not to scale).

FIG. 9 shows a more detailed view of a circulatory assist pump, in accordance with embodiments of the disclosure.

FIG. 10 depicts a belt and controller positioned on a subject that is designed to interact with a circulatory assist pump within the subject, in accordance with embodiments of the disclosure.

FIG. 11 depicts a physiologically accurate mock circulation loop, in accordance with embodiments of the disclosure.

FIG. 12 depicts a “Biomerics Advanced Catheter” having a catheter, catheter connector, drive shaft, handle, impeller, stent cage, and tip, in accordance with embodiments of the disclosure.

FIG. 13 depicts a front view of a stent cage of a circulatory assist pump showing the highly open design of the cage, in accordance with embodiments of the disclosure.

FIG. 14 depicts another circulatory assist pump, in accordance with embodiments of the disclosure.

FIG. 15 depicts another circulatory assist pump with deployed impellers encaged within the stent cage at the tip of the catheter to the right of its associated cross-sectional view taken along lines A-A, in accordance with embodiments of the disclosure.

FIG. 16 depicts a wireless circulatory assist pump, in accordance with embodiments of the disclosure.

FIG. 17 depicts the tip of a deployment catheter for the deployment of the wireless circulatory assist pump of FIG. 16 .

FIG. 18 depicts the tip of a retrieval catheter for the removal of the wireless circulatory assist pump of FIG. 16 .

DETAILED DESCRIPTION

In the Brief Summary above and in the Detailed Description, the claims below, and in the accompanying drawings, reference is made to particular features (including method acts) of the present disclosure. It is to be understood that the disclosure includes all possible combinations of such particular features. For example, where a particular feature is disclosed in the context of a particular embodiment, or a particular claim, that feature can also be used, to the extent possible, in combination with and/or in the context of other particular aspects and embodiments described herein.

The use of the term “for example,” means that the related description is explanatory, and though the scope of the disclosure is intended to encompass the examples and legal equivalents, the use of such terms is not intended to limit the scope of an embodiment or this disclosure to the specified components, acts, features, functions, or the like.

Drawings presented herein are for illustrative purposes only, and are not meant to be actual views of any particular material, component, structure, or device. Thus, embodiments described herein are not to be construed as being limited to the particular shapes or regions as illustrated, but include deviations in shapes that result, for example, from manufacturing. For example, a region illustrated or described as box-shaped may have rough and/or nonlinear features, and a region illustrated or described as round may include some rough and/or linear features. Moreover, sharp angles that are illustrated may be rounded, and vice versa. Thus, the regions illustrated in the figures are schematic in nature, and their shapes are not intended to illustrate the precise shape of a region and do not limit the scope of the present claims. The drawings are not necessarily to scale. Additionally, elements common between figures may retain the same numerical designation.

As used herein, the term “configured” refers to a size, shape, material composition, material distribution, orientation, and arrangement of one or more of at least one structure and at least one apparatus facilitating operation of one or more of the structure and the apparatus in a predetermined way.

As used herein, the singular forms “a,” “an,” and “the” include the plural forms as well, unless the context clearly indicates otherwise.

As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.

As used herein, relational terms, such as “first,” “second,” etc., are used for clarity and convenience in understanding the disclosure and accompanying drawings and does not connote or depend on any specific preference, orientation, or order, except where the context clearly indicates otherwise.

As used herein, the term “about,” when used in reference to a numerical value for a particular parameter, is inclusive of the numerical value and a degree of variance from the numerical value that one of ordinary skill in the art would understand is within acceptable tolerances for the particular parameter. For example, “about,” in reference to a numerical value, may include additional numerical values within a range of from 90.0 percent to 110.0 percent of the numerical value, such as within a range of from 95.0 percent to 105.0 percent of the numerical value, within a range of from 97.5 percent to 102.5 percent of the numerical value, within a range of from 99.0 percent to 101.0 percent of the numerical value, within a range of from 99.5 percent to 100.5 percent of the numerical value, or within a range of from 99.9 percent to 100.1 percent of the numerical value.

As used herein, the term “substantially” in reference to a given parameter, property, or condition means and includes to a degree that one of ordinary skill in the art would understand that the given parameter, property, or condition is met with a degree of variance, such as within acceptable tolerances. By way of example, depending on the particular parameter, property, or condition that is substantially met, the parameter, property, or condition may be at least 90.0 percent met, at least 95.0 percent met, at least 99.0 percent met, at least 99.9 percent met, or even 100.0 percent met.

As used herein, the terms “biocompatible material” and “biocompatible materials” include any materials suitable for being within a subject's (e.g., a mammal's, such as a human's) body. Biocompatible materials include ceramics and ceramic composites such as alumina (Al₂O₃), zirconia (ZrO₂), hydroxyapatite (Ca₁₀(PO₄)₆(OH)₂), and bioglass (e.g., composites including silica (SiO₂), calcium (Ca), sodium oxide (Na₂O), hydrogen (H), and/or phosphorous (P)). As non-limiting examples, bioglass may include 45S5 (e.g., 45% SiO₂, 24.5% CaO, 24.5% Na₂O, and 6% (P₂O₅) and additional compositions described in the following article, the contents of which are incorporated herein by this reference: Bioglass: A novel biocompatible innovation, Vidya Krishnan and T. Lakshmi, Journal of Advanced Pharmaceutical Technology & Research, Volume 4(2), Apr-Jun 2013, pages 78-83, DOI: 10.4103/2231-4040.111523. Biocompatible materials may additionally include metals and metal alloys, such as stainless steel, titanium and titanium alloys (e.g., Nitinol), cobalt-chromium alloys (e.g., ASTM F75). Furthermore, biocompatible material may include polymers, such as polyvinylchloride (PVC), polyethylene (PE), polypropylene (PP), polytetrafluoroethylene (PTFE), polymethylmethacrylate (PMMA), trimethylcarbonate (C₄H₆O₃), TMC NAD-lactide (CH₃[C₆H₈O₄]_(m)[C₄H₆O₃]_(n)CH₃), polylactic acid (PLA), and medical-grade silicone.

FIGS. 1-4 illustrate an impeller 10 of a circulatory assist pump, in accordance with embodiments of the disclosure. FIGS. 1, 3, and 4 shows the impeller 10 of a circulatory assist pump 100 (see FIG. 16 ) in a deployed (e.g., operational) position, and FIG. 2 shows the impeller 10 in a stowed (e.g., collapsed) position. The impeller 10 generally includes a tubular elongated casing 12 associated with a pair of arm-like impeller blades 14, 16. The depicted impeller blades may be pivotally associated with the remainder of the lobe by pivots (e.g., pins or shafts) 11 placed in apertures 13 in the tubular elongated casing 12 and impeller blades. The impeller blades 14, 16 may be outwardly foldable and retractable, and can move, e.g., into a position perpendicular to the tubular elongated casing 12. The impeller 10 may transition between the stowed position, in which the impeller blades 14, 16 are parallel to and within the tubular elongated casing 12, and the deployed position, in which the impeller blades 14, 16 are perpendicular to the tubular elongated casing 12.

The depicted impeller 10 includes a positioning cable 18 running along the impeller axis, about which the impeller blades 14, 16 (along with the rest of the device) rotate to create a pump action, for example, in the aorta. The arm-like nature of the depicted impeller blades 14, 16 allows them to extend maximally from the remainder of the body when in a perpendicular position and fill a large portion of the descending aorta. At the end of the positioning cable is a rod 20 that interacts with a cam portion 22 of each impeller blade (see, e.g., FIGS. 4 and 6 ). Advancing (or relatively displacing) the rod 20 such that the rod abuts and actuates the cam portion 22 causes the impeller blades 14, 16 of the withdrawn impeller (FIG. 3 ) to extend outwards from the rest of the lobe (FIG. 1 ). The cam lobe design (FIG. 4 ) is utilized to expand and retrieve the impeller into and out of the catheter, which is far more reliable deployment than with, for example, a spring design, although a spring may also be used herein. For example, springs vary with temperature and manufacturing, while cam lobes are consistent and remain constant.

As depicted in FIGS. 5 and 6 , each impeller blade 14, 16 has a tip 24, face 26, and back 28 (any or all of which may be magnetic so as to be driven by a wireless drive). The impeller blade 14, 16 shape design as depicted in FIGS. 5 and 6 maximizes blood flow at low power/lower RPMs, while reducing hemolysis and heat. Lower RPMs mean less power needs, improving a system powered wirelessly. There is also reduced risk of a mechanical breakdown. Materials that can be magnetized, which are also the ones that are strongly attracted to a magnet, are called ferromagnetic (or “ferrimagnetic”). Such materials include iron, nickel, cobalt, some alloys of rare-earth metals, and some naturally occurring minerals.

In certain embodiments, the impeller blades can be tilted on demand (in the same manner as the way an airplane wing flaps are controlled) by, e.g., adjustment of the cams, which balances hemolysis, thrust, and flow; maximizes flow with a temporary increase in hemolysis; and can be used to catch native aortic flow to re-charge a battery in the center spindle.

An aortic stent cage surrounds the impeller (see, e.g., FIGS. 9 and 12-16 ) and preferably has the most open area possible (see, e.g., FIG. 13 ), so as to reduce hemolysis. The system thus matches greater strength and protection in balance. The wire-like elements of the stent cage are preferably rounded and are not too thin (like razor wire that can cut blood cells) or too thick like the prior art's flat elements, which can smack hard against and damage blood cells (hemolysis) on their flat surface planes. The depicted aortic stent protective cage with high flow through areas has rounded elements and balance stability strength with low hemolysis and high flow. Preferably, the aortic stent has strength and not too many flat cage elements to damage blood cells and inhibit flow. This may be achieved by use of the rounded cage elements and by design permitting high radial force and strength (certain prior art devices do not even reach the aortic wall (e.g., <20 mm in an adult human) and bounce back and forth in large aortas).

Prior art devices have been known to migrate up and down and bounce side to side in the aorta. Their flow is disturbed and energy is lost in the process. Their movement causes turbulence, which promotes blood clotting and hemolysis.

An aortic stent as described herein (see, e.g., FIG. 15, 16 ) can be detached from the associated drive shaft and external motor controller (which are removed from the subject) and can be converted to wireless power. For example, instead of being driven by the drive axis, the pump can then be powered via, e.g., an external belt system or wireless power WiFi in the subject's home or workplace.

The system is preferably positioned and stabilized in the aorta and the available impeller space is widened with a high radial force aortic stent that distends the aortic wall inner diameter, for example, about two (2) mm. Such positioning allows more flow and more use of the entire area of the aorta, particularly in comparison to the prior art. Such aortic stent strength stabilizes position and reduces the need for repositioning.

In preferred embodiments, a confirming high radial force aortic stent provides for firm stability of fixation of position without the need for hooks. Such a system distends the diameter of the aorta by about two (2) mm (on average), which provides more space available for impeller use.

The expandable stent may be manufactured and adapted for use herein in accordance with techniques known by those of skill in the art (see, e.g., U.S. Pat. No. 5,354,308 to Simon et al. (Oct. 11, 1994), U.S. Pat. No. 4,580,568 to Cesare Gianturco (Apr. 8, 1986), and U.S. Pat. No. 5,957,949 to Leonhardt et al. (Sep. 28, 1999), the contents of each of which are incorporated herein by this reference).

In certain embodiments, the catheter protective cage aortic stent expands and compresses easily, e.g., to pass another catheter by the stent cage. For example, a standard PCI catheter was run up the outside of the stent cage and was of no issue. The radial force of the stent is insufficient to collapse the PCI catheter, particularly when placed against a compliant aorta. The stent typically presses the PCI catheter about 1 mm into the aorta wall and leaves open the whole aorta for the impeller with a large safety gap. The impeller may be angled down like arrow feathers, and then there is even more room for placing a PCI catheter.

The protective cage opens and closes relatively easily with a simple turn of the wheel on a handle associated with the catheter (FIG. 12 ). Collapsing it partially (or fully) allows for the passage of the PCI catheter and then may be opened up fully when the PCI catheter is in place.

As best depicted in FIG. 13 (a front view of the stent cage), the (aortic) stent cage is preferably designed with a highly open flow to prevent damage to, e.g., the subject's blood cells, such as hemolysis and also reduces the risk of thrombosis.

In certain embodiments (e.g., to reduce the chance that the impeller impacts the stent cage on the side where the PCI catheter is present), the impeller is not extended all of the way (e.g., instead of opening it 11.5 mm wide in a 22 mm aorta, it is only opened, e.g., 8 mm wide, but it still provides 80 to 90% of the flow as compared to when the impeller blades are fully open).

In certain embodiments, the impeller is first started turning with the blades, e.g., only half way open, and after it has been confirmed (e.g., either by measuring flow, viewing the situation, or otherwise) that sufficient gap space exists in the aorta, then the impeller is, e.g., fully opened. This serves to allow one to pump in smaller aortas. A half open impeller diameter is only about 8 mm, while fully open may be, e.g., 11.5 to 18 mm depending on size. Only about 20% of the flow is lost at “half open” in comparison to full open. In some test cases, the flow at “half open” was equal to the flow at full open in animal studies at Tufts Medical Center.

In certain embodiments, magnetized impeller blade tips may be powered wirelessly by an external power belt (electrically powered with a copper coil inside) place around, e.g., the subject's abdomen. Wireless power enables the system to provide the subject with a better quality of life, while reducing the risk of infections and providing the physician with greater subject management options. Wireless power systems are disclosed in, e.g., J. Bowler, “This Wireless Heart Pump Battery Could Save Thousands of Lives” ScienceAlert (May 26, 2017) and Knecht et al., “High Efficiency Transcutaneous Energy Transfer for Implantable Mechanical Heart Support Systems” (Nov. 2015); DOI: 10.1109/TPEL.2015.2396194, the contents of each of which are incorporated herein by this reference. Such a transcutaneous energy transfer system (“TETS”) may be used, e.g., with a ventricular assist device. A TETS system setup includes a power converter, rectifier, and coils. See, also, Ho et al., “Midfield Wireless Powering for Implantable Systems,” Proceedings of the IEEE, pp. 1-10 (2013 IEEE), the contents of which are also incorporated herein by this reference.

In certain embodiments, WiFi power may be used to control and power the device/system (with WiFi power) instead of using a belt. In such embodiments, repeater, booster, and/or extender technology, may be used with an external wireless power belt to reduce irritation and heating of, e.g., the subject's skin. See, e.g., “WiFi Boosters, Repeaters and Extenders,” RepeaterStore (repeaterstore.com/pages/wifi-booster-repeater-extender-differences) (accessed Feb. 26, 2018), the contents of which are incorporated herein by this reference. The system preferably utilizes wireless repeater power with minimal skin irritation. See, also, D. Gershgorn, “Your Wireless Internet Could Power Your Future Devices,” Popular Science (popsci.com/your-wireless-internet-could-power-your-future-devices) (Jun. 3, 2015), and J. Langston, “Popular Science names ‘Power Over Wi-Fi’ one of the year's game-changing technologies,” UW News, (washington.edu/news/2015/11/18/popular-science-names-power-over-wi-fi-one-of-the-years-game-changing-technologies/) (Nov. 18, 2015), the contents of each of which are incorporated herein by this reference.

Wireless control of the system can also be used to promote expression of desirable protein(s) via, e.g., implanted micro coils on the stent. See, e.g., US Patent publication US 2017/0266371 A1 to Leonhardt et al. (Sep. 21, 2017), the contents of which are incorporated herein by this reference, for protein expression signals. These micro coils too can utilize wireless energy. Wireless control can extend to pulsatility, speed, and/or impeller angle of the various components of the system. The micro coils can be utilized to control release and/or expression of protein(s) in the aorta, including the release and/or expression of elastin to improve the elasticity of the aorta and mediate stem cell homing and the release and/or expression of follistatin to build new, strong, thick smooth muscle.

The pump may be placed, for example, above the renal arteries in the aorta to aid in kidney function. More flow into the kidneys means more rapid removal of excess fluids, which leads to better revival of kidney function. In certain embodiments, the system preferably uses the full diameter of the aorta to increase pump stability and reduce pump migration.

In animal studies using the described system in sheep and swine, 1.5 to 2.0 liters of true augmented blood (beyond native cardiac output) were provided. With direct flow cannulas placed into the kidneys, the system able to augment renal blood flow by 25 to 50%. The pump was able to generate a gradient of more than 10 mm to unload the left ventricle and achieve improved hemodynamics without any clinically significant steal (reversed flow in the artery). Further, there was a reduced cardiac work index. There was also a significant increase in urine output and no significant hemolysis.

Indications for use of the described system include cardio-renal syndrome, protecting renal function during PCI, and chronic heart failure.

The outwardly foldable impeller uses rotational motion to draw blood in and down from the heart, and moves the blood down the aorta while itself remaining stationary due to the positioning of the cage stent within the aorta. In certain embodiments, controls (e.g., wireless controls) are utilized to modify the rotating impeller blade angles in order to, for example, change flow characteristics. This can be used, e.g., in short durations to dramatically increase flow at the expense of temporary increase of hemolysis, but the system can revert back to a low hemolysis angle shortly thereafter.

The impeller maximizes blood flow, while minimizing hemolysis, power needs, RPMs, and turbulence. The system preferably uses the least RPMs and highest flow and thus lowest hemolysis. The use of a simple impeller lowers the risk of mechanical failure.

Wireless technology can also be used to re-charge a battery or back up a battery for the system as needed.

In one embodiment (not shown), a battery backup power source is housed in the center spindle of the circulatory assist pump, which battery backup power source can be charged either by impeller blade turns or by wireless external recharging.

In certain embodiments, wireless power also powers the turns of the magnetized impeller blades directly, and battery power is only used as a backup.

In certain embodiments, the system includes implanted sensors that assist with a real time, automatic adjustment and management of the circulatory assist support system based upon data provided by the implanted (preferably wireless) sensors. The sensors monitor fluid flow and provide feedback and data to the system, which feedback and data is used to, e.g., adjust the speed and/or angle of the impeller to increase or decrease fluid flow and pressure.

Sensor(s) monitor hemolysis levels and automatically adjust the balance of RPM speed of the impellers and the pulsations of the cuffs (if present), to balance the minimization of hemolysis with the maximization of flow efficiency.

In certain embodiments, the system includes means for synchronous pumping, which is determined by the sensors. See, e.g., Gohean et al., “Preservation Of Native Aortic Valve Flow And Full Hemodynamic Support With The TORVAD™ Using A Computational Model Of The Cardiovascular System,” ASAIO J. 2015 May-Jun; 61(3): 259-265; doi: 10.1097/MAT.0000000000000190, the contents of which are incorporated herein by this reference.

The range of blood flow parameters in the ascending aorta that can result from various angulations of outflow graft anastomosis of a left ventricular assist device (“LVAD”) to the aortic wall, have been quantified as a means to understanding the mechanism of aortic valve insufficiency. See, e.g., Callington et al., “Computational fluid dynamic study of hemodynamic effects on aortic root blood flow of systematically varied left ventricular assist device graft anastomosis design,” J. Thorac. Cardiovasc. Surg. 2015 Sep;150(3):696-704. doi: 10.1016/j.jtcvs.2015.05.034. Epub 2015 May 15, the contents of which are incorporated herein by this reference.

Thus provided is the automatic adjustment of the impeller speed and pulsations of the pulsating cuff based upon real time pressure differentials and other data from the implanted sensors, which are placed in strategic positions. In a preferred embodiment, the sensors are placed above and below the catheter, cuffs, or stents. Such an embodiment optimizes flow by also timing pulsations of the pulsating cuff and impeller speed/angle with subject conditions and needs, including synchronization thereof with optimal real time pulsatile flow.

With various prior art devices, clinicians need to make manual adjustments of up to a dozen times an hour around the clock to be able to manage circulatory assist support based upon a chosen constant aortic pressure differential range or other sensing parameters. In contrast, the described system can be managed automatically and more frequently with the intention of improving subject outcomes. Furthermore, in designing a wireless power-based system and taking into consideration the risk of mechanical breakdown, demands on the system can be reduced (when subject conditions permit) for a time, allowing the device to “cool off” or “rest.” Inversely, the circulatory assist support can be turned up when demands dictate a genuine need and not before.

Such a system permits subject treatment to be customized on a real time personalized basis to provide superior outcomes for subjects (e.g., those suffering from cardio-renal dysfunction in the advanced stages of heart failure).

In one embodiment of the system, a first impeller stent pump is positioned in the subject's ascending thoracic aorta, which unloads blood from the subject's heart (e.g., the first impeller stent pump is positioned to withdraw blood from the subject's left ventricle). In such an embodiment, a pulsating, partially ePTFE (expanded polytetrafluoroethylene) covered stent graft with three (3) pulsating bands is preferably positioned in the aorta downstream from the positioned first impeller stent pump. Also, a second impeller stent pump is positioned further downstream in the subject's descending aorta, just above the subject's renal arteries.

Such a three (3) band pulsating aortic stent graft typically a stent made of flexible compliant material (like an intra-aortic balloon pump (“IABP”) catheter balloon turned inside out). Two of the bands are always firmly against the aorta wall and only one band squeezes inward into the aorta at a time.

Left ventricular unloading is known and described, e.g., in Watanabe et al., “Left Ventricular Unloading Using an Impella CP Improves Coronary Flow and Infarct Zone Perfusion in Ischemic Heart Failure,” J. Am. Heart Assoc. 2018; 7:e006462. DOI: 10.1161/JAHA.117.006462, Esposito et al., “Left Ventricular Unloading Before Reperfusion Promotes Functional Recovery After Acute Myocardial Infarction,” Journal of the American College of Cardiology, Vol. 72, issue 5, pp. 501-514 (Jul. 31, 2018), Saku et al., “Total Mechanical Unloading Minimizes Metabolic Demand of Left Ventricle and Dramatically Reduces Infarct Size in Myocardial Infarction,” doi.org/10.1371/journal.pone.0152911 (2016), Kapur et al., “Mechanically Unloading the Left Ventricle Before Coronary Reperfusion Reduces Left Ventricular Wall Stress and Myocardial Infarct Size,” Circulation. 128. 10.1161/CIRCULATIONAHA.112.000029. (June 2013), dx.doi.org/10.1161/CIRCULATIONAHA.112.000029, and “Acute Cardiac Unloading and Recovery,” Interventional Cardiology Review 2017; 12(2 Suppl 2):1-28. See, also, Esposito M L, Kapur N K. “Acute mechanical circulatory support for cardiogenic shock: the ‘door to support’ time,” F1000Research. 2017;6:737. doi:10.12688/f1000research.11150.1.

The real time auto adjustment technology should serve subjects, such as those that have physiologic hemodynamic changes due to things as simple as sleep and exercise with advanced heart failure changes in edema levels and modulation of the pump thrust, volume and impeller speed may serve these subjects well. By enabling real time automatic adjustments of circulatory assist pump controls to adjust to the constant turbulent changes in hemodynamic and edema conditions that occur on an ongoing basis in, e.g., advanced heart failure subjects.

A preferred aortic stent cage is designed to minimize hemolysis, while maximizing flow and stability. It is designed to avoid thick elements and to avoid razor cutting. It maximizes stability and positioning of the system. It presently serves as the best protection against the impeller blade(s) hitting the aortic wall.

The wire diameter of the stent cage circulatory assist catheter should be from about 0.015 to about 0.022 inches; preferably about 0.018 inches. Such a diameter is not too thin to cut blood cells and not too thick to ram them hard damaging them.

The catheter and drive shaft are designed to reduce risk of mechanical breakdown by having fewer bearings, which requires less fluid lubrication and flush. They are also designed to ease placement and minimize FR size. The drive shaft lubrication system preferably has minimal bearings and utilizes liquid cooling and an expanded polytetrafluoroethylene (“ePTFE”) liner. ePTFE is commercially available from, e.g., W.L. Gore & Associates.

Preferably, the impeller rotates at a number of revolutions, which is less than 10,000 rpm, preferably on the order of 4,500 rpm. Lower RPMs reduce the risk of mechanical failure and also reduce power needs. This can be important since, as reported by Kormos et al., “Left Ventricular Assist Device Malfunctions: It's More Than Just The Pump,” CIRCULATIONAHA.117.027360, originally published Jul. 3, 2017 (doi.org/10.1161/CIRCULATIONAHA.117.027360), 19% of subjects suffered battery failure with the Heartmate II over 3 years. Heartmate II (Thoratec Corporation) is a heart pump called a left ventricular assist device (LVAD), which was designed to assist the left side of the heart to pump the blood a body needs. Furthermore, 21% of the HeartMate II subjects were reported to have had driveline failure with the HeartMate II. The herein described preferred device having liquid cooled, minimal bearing system with ePTFE line and hydrophilic coated drive shaft act to reduce driveline failures.

As depicted in FIG. 8 , a circulatory assist system generally includes a motor and controller, a catheter (e.g., a Biomerics Advanced Catheter from Biomerics, Brooklyn Park, Minn.) that includes the catheter, catheter connector, drive shaft, handle, propeller/impeller, and tip, and a stent cage or frame, e.g., adapted through laser welding for application. As shown in FIG. 14 , a “Biomerics Advanced Catheter” has a catheter handle, catheter connector, drive shaft, impeller encaged within the stent cage, and catheter tip.

A preferred handle (FIG. 12 ) typically has two wheels to manipulate the impeller and deployment of the stent. The first wheel may thus be used to remove the sheath and expose the (closed) impeller pump. The stent typically has a diameter of 20 mm, while the “opened” device typically has a diameter of 22 mm.

In FIG. 8 , the propeller-driven “pump” includes a driveline (“sheath”) and the impeller. A proximal sheath is a driveline connecting the pump to a handle (or distal sheath/driveline). The distal driveline connects to a console motor (e.g., depicted is a light and quiet external BLDC motor that is mechanically and thermally isolated and uses a flexible interconnect for ease of positioning, a motor drive control unit and central alarm box). A console extension cable may be used to connect the console to the motor. The console thus may control operation of the pump by controlling the rotation of the impeller. An infusion pump (the one depicted in FIG. 8 is an off the shelf IVAC/Infusion pump system using standard infusion tubing that terminates in a male Luer connector; medical grade UPS for transport and system power back up) may be used to control the volume of fluid entering the pump (above the distal sheath/driveline). The depicted distal and proximal sheath drivelines use Nitinol inner shafts, a positive action handle for accurate deployment, retraction, and locking of impeller blades. Infusion tubing is then used to deliver fluid as desired.

Such a system can generally involve two different embodiments. First, the temporary circulatory assist support pump(s) is/are placed on the tip of endovascular aortic catheter. Second, the system may include a removable chronic wireless powered implant circulatory assist pump within an aortic stent.

Such a system is designed to reduce heart work load and improve perfusion, improve renal function, normal the hemodynamics of acute decompensating heart failure subjects, support heart regeneration procedures, help subjects recover from cardiogenic shock, reduce risks associated with percutaneous catheterization interventions (“High Risk PCI”), help subjects on the amputation list. Such a system is designed to reduce end diastolic pressure and to reduce end diastolic volume. It is further designed to reduce oxygen demand of myocardium.

Such a system utilizes a relatively straightforward aorta position insertion and is relatively stable over time. It promptly provides hemodynamic support. It is designed to minimize heart valve damage and to minimize coronary re-perfusion injury. It is designed to have low shear stress on blood, and minimize hemolysis.

The wireless power embodiment is designed to reduce infection risk compared to external drive line systems. Also, the wireless power option helps improve the subject's quality of life.

Preferably, the system is utilized with an upper aorta pulsating aortic cuff stent graft, which improves the total flow of the system, improves hemodynamics, (via the pulsatile flow) improves the release of beneficial proteins for organ health, and reduces RPMs needed by the impeller to reach desired flow rates. A preferred system includes at least three (3) pulsating aortic cuffs on a flexible mesh aortic stent. Pulsating cuffs placed on the top, middle, and bottom of a flexible mesh stent may be controlled via an external abdominal belt.

Pulsating electromagnetic waves may be, e.g., delivered non-invasively from an abdominal belt (e.g., FIG. 10 ) in direct communication with the aortic blood flow.

In certain embodiments, the wirelessly driven impeller is contained within a high aortic force protective cage stent is placed within such an upper aorta pulsating aortic cuff stent graft in the subject.

The system preferably combines the upper aorta pulsating aortic stent graft with a lower aorta impeller pump within a bare aortic stent to optimize flow with the least power and the least RPMs. Other pulsating aortic stent grafts are on the outside of the aorta, while the described is preferably on the inside. This is more effective, with less variability

In some embodiments, a wireless circulatory assist pump includes a wirelessly driven impeller contained within a protective aortic cage stent. The wireless circulatory assist pump may include a cam lobe to release and retract the shaped impeller (e.g., 14.5 mm width) blades, two bearings, and an open protective aortic cage stent. The elements of the protective aortic cage stent are rounded. Wireless circulatory assist pumps may utilize relatively low RPM speed (7,500 vs. 10,000 to 33,000 RPM), maintain arterial pulsatility, and preferably use the entire diameter of the aorta of the subject (with the use of a protective aortic cage stent of, e.g., 23.5 mm).

In some embodiments, such as that shown in FIG. 16 , a wireless circulatory assist pump 100 is configured to be inserted into and removed from a vein or artery (e.g., the aorta) via one or more catheters (see, e.g., FIGS. 17-18 ). In FIG. 16 , the depicted wireless circulatory assist pump 100 comprises a first portion 102 at a first end (e.g., a distal tip end), a second portion 104 at a second end (e.g., a proximal docking end), an impeller 106 connected to the first portion 102 and the second portion 104, and a stent cage 108 between and connected to the first portion 102 and the second portion 104 of the wireless circulatory assist pump 100. The impeller 106 may include a drive shaft or axle, and may also be enclosed within a stent cage 108 therebetween.

The second portion 104 of the wireless circulatory assist pump 100 may be configured to connect (e.g., removably connect) to a catheter for placement and removal of the wireless circulatory assist pump 100 within a subject. Accordingly, when the circulatory assist pump 100 is positioned within a subject, the second portion 104 may be distal from the subject's heart, and the first portion 102 may be proximate to the subject's heart.

The wireless circulatory assist pump 100 may further comprise a battery 110, circuitry 112, and a motor 114. The circuitry 112 may comprise a wireless charging circuit, a communications circuit, and a control circuit. The motor 114 is operably coupled to the impeller 106 to transfer power and drive the impeller 106. As shown in FIG. 16 , the battery 110, the circuitry 112, and the motor 114, may be housed within the first portion 102 of the wireless circulatory assist pump 100. While the battery 110, the circuitry 112, and the motor 114 are shown as being housed within the first portion 102 of the wireless circulatory assist pump 100, it will be understood that one or more, or all, of the battery 110, the circuitry 112, and the motor 114, may alternatively be housed within the second portion 104 of the wireless circulatory assist pump 100.

The first portion 102 of the wireless circulatory assist pump 100 may comprise have a smooth, rounded exterior surface, and a distal end of the first portion 102 (e.g., furthest from the stent cage 108 and/or the second portion 104 of the wireless circulatory assist pump 100) may exhibit a dome shape. This may inhibit (e.g., prevent) harm to a subject, if the distal end of the first portion 102 comes into contact with the arterial wall of the subject, such as during insertion of removal of the wireless circulatory assist pump 100. The first portion 102 may comprise a canister covering and sealing the components (e.g., the battery 110, the circuitry 112, and the motor 114) housed within the canister. For example, the canister may be hermetically sealed. In some embodiments, the first portion 102 comprises a biocompatible ceramic portion surrounding the circuitry, and a biocompatible polymer and/or biocompatible metal portion surrounding the battery and the motor. The ceramic portion surrounding the circuitry may facilitate electromagnetic, electric, and/or magnetic communication between devices located outside of the subject's body and the circuitry 112 within the first portion 102 of the circulatory assist pump 100.

In some embodiments, as shown in FIG. 16 , the first portion 102 of the wireless circulatory assist pump 100 includes the battery 110 at a distal end of the first portion 102 (e.g., furthest from the stent cage 108 and/or the second portion 104 of the wireless circulatory assist pump 100), the motor 114 at a proximal end of the first portion 102 (e.g., closest to the stent 108 and/or the second portion 104 of the wireless circulatory assist pump 100), and the circuitry 112 interposed between the battery 110 and the motor 114. In additional embodiments, the position of the circuitry 112 and the battery 110 may be switched, such that the circuitry 112 is at a distal end of the first portion 102, and the battery 110 interposed between the circuitry 112 and the motor 114.

The placement of the battery 110, the circuitry 112, and the motor 114 within the first portion 102 of the wireless circulatory assist pump 100 may result in a first mass of the first portion 102 being greater than a second mass of the second portion 104 of the wireless circulatory assist pump 100. For example, a ratio of the second mass of the second portion 104 to the first mass of the first portion 102 may be within a range of from about 50:1 to about 1:1, such as from about 20:1 to about 1.5:1, from about 15:1 to about 2:1, from about 12:1 to about 3:1, or from about 8:1 to about 4:1. The first portion 102 having a greater mass than the second portion 104 may inhibit and/or prevents positional movement by impact (e.g., jumping). This configuration may also increase the radial force applied by the stent cage 108 to the aortic walls of a subject, when the wireless circulatory assist pump 100 is deployed within the subject. In additional embodiments, the second mass of the second portion 104 of the wireless circulatory assist pump 100, may be greater than the first mass of the first portion 102 of the wireless circulatory assist pump.

The motor 114 may be a miniature brushless direct current (DC) motor. For example, the motor 114 may be a miniature brushless DC motor such as available under the tradename “EC6” from Maxon Precision Motors, Inc. of Foster City, Calif. USA.

The battery 110 may be a rechargeable battery, such as a lithium-ion battery. For example, the battery 110 may be a 3 milliamp hour (mAh) lithium-ion battery available under the tradename “CONTIGO” from EaglePicher Technologies of Joplin, Mo. USA. For another example, the battery 110 may be a 3 mAh lithium-ion battery available under the tradename “MICRO3-QL0003B” from Quallion LLC of Sylmar, Calif. USA. It will be understood, however, that the battery 110 may be of any suitable chemistry and/or type, including non-chemical electric power storage devices, such as a capacitor (e.g., a supercapacitor, ultracapacitor, or double-layer capacitor).

The circuitry 112 is typically sealed in an RF translucent material such as ceramic, ePTFE, or Polyether ether ketone (“PEEK”) (so as not to block RF), and may comprise a wireless charging circuit (e.g., an inductive charging coil), a communications circuit, and a control circuit.

In some embodiments, the wireless circulatory assist pump 100 may comprise one or more application-specific integrated circuit (“ASIC”) chips. For example, one or more of the charging circuit, the communication circuit, and the control circuit may include one or more ASIC chips.

The wireless charging circuit may be in electronic communication with the control circuit, the communications circuit, the battery 110, and the motor 114. The wireless charging circuit may produce an electric current in response to an applied electric field, magnetic field, and/or electromagnetic field, which may be utilized to charge the battery 110, power the motor 114, and provide power to the communication circuit and the control circuit. For example, the wireless charging circuit may comprise an induction coil and/or an antenna, and energy may be transferred to the wireless charging circuit via inductive coupling (e.g., resonant inductive coupling) and/or electromagnetic waves (e.g., radio waves). Although a “puck” receiving coil might be utilized, a “puckless” TET is preferably used, which coil comprises a high permeability, ferromagnetic core with a high Q RF coil (miniaturized receiving coil) positionable inside of the distal tip of the wireless circulatory assist pump 100. See, e.g., Loeb et al., “Bion system for distributed neural prosthetic interfaces,” Medical Engineering and Physics, 23(1):9-18, Jan. 2001; U.S. Pat. No. 7,005,935 to Moore (Feb. 28, 20206) for “Switched reactance modulated E-class oscillator.” The resulting lack of wires in the aorta and/or femoral arteries reduces the risk of infection.

Preferably, ultralow power magnetic induction power transmission is used to power and control such a wireless circulatory assist pump 100. This results in truly wireless operation, with little to no heat generation. The system utilizes a low frequency design with extremely conservative operating frequencies and extraordinarily low specific absorption rate (SAR) value. SAR is a measure of the rate at which energy is absorbed per unit mass by a human body when exposed to a radio frequency (RF) electromagnetic field. It is defined as the power absorbed per mass of tissue and has units of watts per kilogram (W/kg).

The wireless circulatory assist pump 100 is further preferably configured so that the magnetic flux (or flux area) of the wireless circulatory assist pump 100 accommodates angles of anatomical variability so that the device maintains constant operation.

The communication circuit may be configured to send and receive data via wireless communication. For example, the communication circuit may be configured to send and receive data utilizing radio communication (e.g., WiFi, Bluetooth, etc.). In some embodiments, the communication circuit may be utilized to send data collected from one or more sensors of the wireless circulatory assist pump 100. For example, the communication circuit may be utilized to send data relating to the rotational speed of the pump, upstream and downstream fluid pressures, battery charge status, motor status, impeller status, and/or other measured conditions.

The control circuit may be utilized to control certain operations of the wireless circulatory assist pump 100. In some embodiments, the control circuit may be utilized to control the motor 114 and the impeller 106. For example, the rotational speed of the motor 114, the deployment of the impeller blades 116, the stowing of the impeller blades 116, the tilt/angle of the impeller blades 116, and/or other operations of the wireless circulatory assist pump 100. In additional embodiments, the impeller blades 116 may be manually deployed and collapsed.

In certain embodiments, the wireless circulatory assist pump 100 further includes a sensor 111 or sensors in one or more ends of the wireless circulatory assist pump 100 (e.g., at the distal end of the first portion 102) to measure and preferably report, e.g., blood pressure. Brancato, Luigi et al., “An Implantable Intravascular Pressure Sensor for a Ventricular Assist Device,” Micromachines vol. 7,8 135. 8 Aug. 2016, doi:10.3390/mi7080135. Control of the sensor(s) can be via the ASIC. In such embodiments, the MCAD system can provide auto correction/selection of speed through the internal feedback of the sensors. Built in telemetry can also be used for communications.

The impeller 106 may be similar to the impeller 10 previously shown and described herein with reference to FIGS. 1-6 . The impeller 106 may be configured to change shapes in one or more various ways. The impeller 106 may comprise impeller blades 116 that may be configured to move between a deployed position, as shown, and a stowed position (see FIG. 3 ). The impeller blades 116 may additionally be configured to move to positions between the deployed position and the stowed position (e.g., a partially deployed position). The impeller 106 may also be enclosed within a stent cage 108 to prevent contact between the impeller blades 116 and the arterial (e.g., aortic) wall of the subject inhibit during operation of the wireless circulatory assist pump 100.

The stent cage 108 may be similar to the stent cage 32 described previously herein with reference to FIGS. 14 and 15 . Accordingly, the stent cage 108 may be configured to securely position the wireless circulatory assist pump 100 in a subject's aorta (e.g., by maintaining a radial force against the aortic wall), while maintaining the pulsatility of the aorta. Additionally, the stent cage 108 may be compressed and stowed for placement and removal of the wireless circulatory assist pump 100.

The second portion 104 (e.g., docking portion) of the wireless circulatory assist pump 100 may comprise features configured to connect (e.g., removably) with a catheter. For example, the proximal end of the second portion 104 may be configured to interact with one or more catheter, such as a deployment catheter 130 (FIG. 17 ) and a retrieval catheter 140 (FIG. 18 ). In some embodiments, the second portion 104 may comprise an annular groove 118 located near the proximal end surface of the second portion 104. The proximal end surface may be dished to provide a generally hemispherical indentation 120 in the second portion 104. For example, the end surface may correspond to the geometry (e.g., the shape and/or size) of a deployment and retrieval catheter. In some embodiments, the second portion 104 may comprise a ferromagnetic material.

A system for a wireless circulatory assist pump may be utilized to deploy and retrieve the wireless circulatory assist pump 100 within a subject. For example, the system for the wireless circulatory assist pump 100 may be used to place the wireless circulatory assist pump 100 in a subject's descending thoracic aorta above the subject's kidneys, and also to remove the wireless circulatory assist pump 100 from the subject. The system for the wireless circulatory assist pump 100 includes a deployment catheter 130 (FIG. 17 ), and a retrieval catheter 140 (FIG. 18 ).

The deployment catheter 130 may include an end configured to connect (e.g., removably connect) to the wireless circulatory assist pump 100.

The deployment catheter 130 comprises an outer sheath 132, an inner member 134 within the outer sheath 132, and a plurality of fingers 136 located between (e.g., radially between) the outer sheath 132 and the inner member 134. The inner member 134 may be configured to move axially relative to the outer sheath such that the deployment catheter 130 is configured to transition between a retracted position (not shown) and an extended position (shown in FIG. 17 ). When the deployment catheter 130 is in the retracted position, the inner member 134 and/or the plurality of fingers 136 are entirely within a central opening of the outer sheath 132. When the deployment catheter 130 is in the extended position, at least a portion (e.g., a portion or the entirety) of the inner member 134 and/or two or more fingers 136 extend axially outward from the outer sheath 132, as shown. In some embodiments, the axial movement between the outer sheath 132 and the inner member 134 may be limited such that the deployment catheter includes a fully extended position, and a fully retracted position.

The outer sheath 132 comprises an elongated tubular member that include a central opening (e.g., axial opening) configured to receive the inner member 134 and the plurality of fingers 136. The outer sheath 132 may comprise a biocompatible material (e.g., a biocompatible polymer).

The inner member 134 comprises an elongated cylindrical member having a smaller outer diameter than the central opening of the outer sheath 132. The inner member 134 may comprise a biocompatible material (e.g., a biocompatible polymer, a biocompatible metal). In some embodiments, the inner member 134 comprises a ferromagnetic material.

The fingers 136 may include fixed ends secured to the inner member 134, and free ends opposite the fixed end. The fingers 136 may be thin strips of a flexible material, such as a biocompatible metal material. The free ends of the fingers 136 may be biased radially outward and apart from one another. For example, a portion of each of the fingers 136 may be bent at the fixed end such that the free ends of the fingers 136 are biased radially outward. The fingers 136 may additionally include protrusions 138 at the free ends. The protrusions 138 of the fingers 136 may be configured to be received within the annular groove 118 (FIG. 16 ) of the wireless circulatory assist pump 100 (FIG. 16 ). Although illustrated as spherical elements, the protrusions 138 may exhibit any desired shape. The protrusions 138 may be sized and shaped corresponding to the size and shape of the annular groove 118 (FIG. 16 ). For example, the protrusions 138 may be partial ring-shaped sections, and the ring-shaped protrusions may be combined to form the shape of a ring corresponding to the shape and size of the annular groove 118 (FIG. 16 ) when connected to the circulatory assist pump 100. In additional, the protrusions 138 on the fingers 136 may be magnetic to secure the fingers 136 to a portion (e.g., the second portion 104 of the wireless circulatory assist pump 100 of FIG. 16 ). For example, the protrusions 138 may comprise neodymium (Nd) and/or samarium-cobalt (SmCo).

In some embodiments, the fingers 136 may be equidistantly spaced (e.g., radially) from one another. For example, two fingers may be about 180° apart from one another, three fingers 136 may be about 120° apart from one another, and four fingers may be about 90° apart from one another. In additional embodiments, the fingers 136 may be unevenly spaced (e.g., radially) from one another. For example, two fingers may be about 60° apart from one another, and two additional fingers may be about 150° apart from one another.

To install the wireless circulatory assist pump 100 within a subject, the end of the deployment catheter 130 may be secured to a portion (e.g., the second portion 104) of the wireless circulatory assist pump 100 while external to a subject and then inserted percutaneously through the subject's femoral artery.

When the inner member 134 and the fingers 136 are extended out of the outer sheath 132, the free ends of the fingers 136 are biased radially outward and apart from one another. Each finger 136 may comprise a protrusion 138 at the tip, which may be spaced sufficiently apart (e.g., radially) that the second portion 104 may freely pass between the protrusions 138. Accordingly, the second portion 104 may be positioned adjacent to the inner member 134, and the protrusions 138 may surround the annular groove 118 of the second portion 104.

The outer sheath 132 may then be extended over the inner member 134 and the plurality of fingers 136. As the outer sheath 132 extends over the fingers 136, the outer sheath 132 may force the free ends of the fingers 136 radially inward and the protrusions 138 of the fingers 136 may be positioned within the annular groove 118 of the second portion 104 of the wireless circulatory assist pump 100, and prevent movement of the second portion 104 relative to the inner member 134 and the fingers 136. The blades 116 of the impeller 106 may be placed into a stowed position and the stent cage 108 may be retracted. In some embodiments the blades of the impeller 106 and the stent cage 108 may be withdrawn into the outer sheath 132.

The end of the deployment catheter 130 and the attached wireless circulatory assist pump 100 may then be positioned within a subject to a desired location for deployment of the wireless circulatory assist pump 100. The resilient material of the stent cage 108 may expand to contact the subject's vessel wall and hold the wireless circulatory assist pump 100 in place. Then, the outer sheath 132 may be withdrawn from the fingers 136 and the inner member 134. As the outer sheath 132 is withdrawn, the free ends of the fingers 136 may be biased radially apart and the protrusions 138 of the fingers 136 may be withdrawn from the annular groove 118, disconnecting the deployment catheter 130 from the second portion 104. The deployment catheter 130 may then be removed from the subject with the wireless circulatory assist pump 100 left in place.

The retrieval catheter 140 of FIG. 18 may be substantially similar to the deployment catheter 130 of FIG. 17 . For example, the retrieval catheter 140 may include an outer sheath 142, an inner member 144, and a plurality of fingers 146 located between the outer sheath 142 and the inner member 144. The outer sheath 142 may be substantially similar to the outer sheath 132, the inner member 144 may be substantially similar to the inner member 134, and the plurality of fingers 146, including the protrusions 150 may be substantially similar to the plurality of fingers 136 and the protrusions 138, respectively. The retrieval catheter 140, however, may additionally include a magnetic end 148 positioned at the end of the inner member 144. For example, the magnetic end 148 may comprise a spherical magnet secured to an end of the inner member 144. In some embodiments, the magnetic end 148 comprises neodymium (Nd) and/or samarium-cobalt (SmCo).

To remove the wireless circulatory assist pump 100, the retrieval catheter 140 having an end shown in FIG. 18 may be utilized. The end of the retrieval catheter 140 may be inserted percutaneously through the subject's femoral artery and, and may be secured to a portion (e.g., the second portion 104) of the wireless circulatory assist pump 100 (FIG. 16 ).

When the inner member 144 and the fingers 146 are extended out of the outer sheath 142, the free ends of the fingers 146 may be biased radially outward and apart from one another. Each finger 146 may comprise a protrusion 150 at the tip, which may be spaced sufficiently apart that the second portion 104 may freely pass between the protrusions 150. Accordingly, the inner member 144, and the magnetic end 148 may be positioned adjacent to the second portion 104 of the wireless circulatory assist pump 100. The magnetic end 148 may be positioned adjacent to and attracted to the ferromagnetic material of the second portion 104, and the magnetic end 148 may become seated within the generally hemispherical indentation 120 in the second portion 104 and magnetically coupled thereto. Upon the seating and magnetic coupling of the magnetic end 148 to the second portion 104, the protrusions 150 may surround the annular groove 118 of the second portion 104.

The outer sheath 142 may then be extended over the inner member 144 and the plurality of fingers 146. As the outer sheath 142 extends over the fingers 146, the outer sheath 142 may force the free ends of the fingers 146 radially inward and the protrusions 150 of the fingers 146 may be positioned within the annular groove 118 of the second portion 104 of the wireless circulatory assist pump 100, and prevent movement of the second portion 104 relative to the inner member 144 and the fingers 146. The blades 116 of the impeller 106 may be placed into a stowed position and the stent cage 108 may be retracted from the artery wall. In some embodiments the blades of the impeller 106 and the stent cage 108 may be withdrawn into the outer sheath 142. For example, embodiments that utilize a shape change impeller 106, may have impeller blades 116 with sufficient flexibility that the impeller blades 116 may naturally fold and conform as the impeller blades 116 are withdrawn into the outer sheath 142. The retrieval catheter 140 and wireless circulatory assist pump 100 may then be removed from the subject.

In certain embodiments, the belt, which is to be worn by the subject (see, e.g., FIG. 10 ), is used to control the pulsatile cuff pulsations, provides wireless power to the lower aortic stent impeller, provides, e.g., vibrational harmonic resonant vibrations or other energy to prevent blood clot formation(s) at, e.g., high risk stagnation points, magnetically or by sound wave pulsations grabs blood and moves it with electro-magnetic or sound waves (may reduce 1,500 RPM to reach 4.5 liters flow to 1,000 RPM estimated), and delivers bioelectric signals into tissues and the aorta releasing proteins beneficial to organ and whole body health (note pulsatility also promotes release of beneficial organ health proteins from the aorta and other arteries and tissues).

The removable pulsatile cuff stent may be placed just above the lower impeller aortic stent, which achieves approximately 2 liters per minute flow improvement on its own. The removable pulsatile cuff stent can be designed to push blood up and down or just down by programming the pulsatile elements. The removable pulsatile cuff stent is timed to pulse squeeze in optimization with the heart natural pulsatility. When the pulsatile cuff stent is in place pulsating, the impeller RPM may be reduced to 1,500 RPM to reach 4.5 liters per minute flow (estimated). This cuff placement provides the option for pulsatile flow circulatory assist augmentation.

Pulsatile stent grafts are disclosed in, e.g., Palma et al., “Pulsatile stent graft: a new alternative in chronic ventricular assistance,” Revista Brasileira de Cirurgia Cardiovascular (2013), 28(2):217; dx.doi.org/10.5935/1678-9741.20130031, the contents of each of which are incorporated herein by this reference.

In one embodiment, a pulsatile stent graft may be included within the system, placed mid-aorta, while substantially continuous impeller power is applied in the bare aortic stent in the lower aorta.

Preferred such systems for use herein are described in: Pahlevan and Gharib, “A wave dynamics criterion for optimization of mammalian cardiovascular system,” J. Biomech. 2014 May 7;47(7):1727-32. doi: 10.1016/j.jbiomech.2014.02.014. Epub 2014 Feb 20., Pahlevan and Gharib, “A Bio-Inspired Approach for the Reduction of Left Ventricular Workload,” PLOSone (Jan. 24, 2014): doi.org/10.1371/journal.pone.0087122, Pahlevan and Gharib, “Aortic Wave Dynamics and Its Influence on Left Ventricular Workload,” PLOSone (Aug. 11, 2011); doi.org/10.1371/journal.pone.0023106, U.S. Pat. No. 9,125,655 to Gharib et al. (Sep. 8, 2015) for Correction and Optimization of Wave Reflection in Blood Vessels; U.S. Pat. No. 7,998,190 to Gharib et al. (Aug. 16, 2011) for Intravascular Miniature Stent Pump; U.S. Pat. No. 7,163,385 to Gharib et al. (Jan. 16, 2007) for Hydroimpedance Pump; U.S. Pat. No. 8,092,365 to Rinderknecht et al. (Jan. 10, 2012) for Resonant Multilayer Impedance Pump; U.S. Pat. No. 7,883,325 to Kheradvar et al. (Feb. 8, 2011) for Helically Actuated Positive-Displacement Pump and Method and U.S. Pat. No. 9,125,655 B2 to Phalevan, the contents of each of which are incorporated herein by this reference.

Preferably, the pulsating cuff pump is positioned in the upper aorta of the subject above the stent cage impeller, which is positioned lower in the aorta. Preferably, two aortic stents in series in the aorta, the top aortic stent being fully pulsatile and the bottom aortic stent semi-pulsatile (meaning it turns, but it turns so far away from heart that it does not take away pulsatility, it just accelerates it). This relative positioning of the two pumps maximizes flow while minimizing impeller RPM. The combination of the pulsating cuff aortic stent graft in the upper aorta with the impeller pump/aortic stent in the lower aorta reduces RPMs from, e.g., 4,500 rpm to attain 4.5 liters per minute flow to 1,500 rpm, and provides advantages in terms of hemodynamics, expression of protein(s), and flow not found in either device alone. Less RPMs requires less power, which translates to a system that is easier to power wirelessly. There is also less of a risk of a mechanical breakdown, and less resulting damage to blood cells from hemolysis.

Such a system, may be combined with, e.g., a vibrating harmonic resonant device to reduce and hopefully prevent blood clots, which is “the Achilles' heel” of chronic implants. A harmonic resonant vibration system to reduce blood clots in such a system is described in U.S. Publication No. US 2019/0125932 A1 to Leonhardt et al. (May 2, 2019) for “Preventing Blood Clot Formation, Calcification and/or Plaque Formation on Blood Contact Surface(S)” the contents of which are incorporated herein by this reference. The system may also (or alternatively) utilize an electric charge surface treatment of the implant to further reduce risk of blood clots, calcification, and plaque forming on the device.

In certain embodiments, the system includes a bi-layer magnetic fluid graft that further increases flow without hemolysis (e.g., the system utilizes a magnetic fluid-filled silicon (bi-layer) graft liner placed on the inside of the impeller stent) where the pulsating waves augment aortic flow.

In certain embodiments, the system magnetically “grabs” blood via iron particles in blood and manages flow wave pulses to optimization and flow optimization timing, which further enhances flow without increasing hemolysis. For example, pulsed electromagnetic waves cam be utilized to “grab” the iron in the subject's blood and move it in waves via an external belt.

The system can further include bioelectric coils on the stent to control expression and/or release of protein(s) such as those that build strength of aortic muscle and/or aid in kidney recovery. See, e.g., the earlier incorporated US Patent publication US 2017/0266371 A1 to Leonhardt et al. (Sep. 21, 2017) and/or Macfelda et al. “Bioelectrical signals improve cardiac function and modify gene expression of extracellular matrix components” ESC Heart Failure 2017; 4: 291-300 (published online 30 Jun. 2017); DOI: 10.1002/ehf2.12169, the contents of which are incorporated herein by this reference. Via the system, inflammation and blood pressure can be managed with bioelectric signal protein expressions and membrane potential management. The platform can also be used to aid in the creation and control of smooth muscle formation in the aorta.

In certain embodiments, wireless powered and programmed micro coils are utilized with the system to control aortic tissue protein expressions and to increase smooth muscle mass and to control pulsations of natural aortic muscle, a cellular muscle-based “second heart.” For example, pacing the timed electrical pulse signals may be utilized to trigger contractions of smooth muscle so to make the natural aorta a beating “second heart” optimized with native pulsatile flow.

The wireless powered and programmed micro coils can be further used to control chronic inflammation and blood pressure with real time reads and adjustments.

The system itself preferably utilizes programmed, real-time optimization to manage flow, hemolysis, power, and subject hemodynamics real time. The programming can be configured to change parameters, e.g., with the subject's exercise, sleep, heart failure conditions, etc., including monitoring fluid level in the subject's lungs, etc.

In certain embodiments, the system includes vibrational harmonic resonant tuned technology, which reduces risk of thrombosis (blood clot formations), reduces risk of plaque or calcification formations, increases gas exchanges in aorta, and promotes healthy protein release in aorta. It is relatively easily mounted into the same belt providing wireless power and controlling pulsating implants and micro coils. Including micro coils controls protein expression in the aorta to, e.g., increase elasticity, control blood pressure, improve organ health, and control inflammation

Blood clots have been the “Achilles heel” of many other chronic implant devices. Resonant harmonic vibrational energy technology may be utilized to reduce the risk of this problem. Tuned harmonic resonant vibration may be used to prevent blood clot formation at high risk stagnation points on the device. The harmonic resonance for each high risk stagnation point may be individually customized and stored in a microprocessor. The vibrational energy may be delivered in pulses in a loop hitting each high risk location of the device to prevent a large accumulation of a blood clot, which might develop.

Pulsatility results in healthier hemodynamics, less risk of thrombosis, together with cellular arterial wall protein expression for superior organ recovery and subject well-being. The device described herein combines the best of pulsatile flow with continuous flow. Using pulsatile and continuous flow optimizes hemodynamics and lessens the risk of thrombosis.

In certain embodiments, the system utilizes a motor console for precision performance and low vibration, with flushing built in.

In certain embodiments, BION micro coil implants are incorporated into the system. They may be utilized to release proteins for the heart, aorta, arteries, lungs and kidney health. They also be utilized to provide real time data on performance, flow, pressures etc.

The system can be utilized variously. For instance, as a temporary catheter alone for 6 to 72 hours. As a temporary catheter with removable pulsating cuff stent in series with both removed after use of 6 to 72 hours. The temporary use catheter may be removed, but the pulsating cuff stent may be left in place for chronic long term use. The catheter and drive shaft can be disconnected from the impeller stent, which can then be switched to wireless power on a standalone basis.

In certain embodiments, there are two aortic stent based circulatory assist pumps in series in the aorta, one upper and one lower, the upper one being pulsatile.

In certain embodiments, the impeller stent can be left out/removed, and the pulsating aortic cuff stent left in place.

The device may be removed should the need for the device abate (e.g., upon recovery of the subject). For removing the device, a modified Seldinger technique (or comparable technique) can be applied in reverse utilizing a catheter that interacts with, e.g., the pump for removal. The impeller blades may first be retracted and the stent cage then collapsed about it to reduce the cross-sectional diameter of the pump to aid in removal.

The foregoing can be supported with a vibrational harmonic resonance technology for preventing blood clot formations (thrombosis), but this is especially preferred when the system is used for chronic implant use. Furthermore, the foregoing can be supported with the release of bioelectrically controlled release of protein(s) from, e.g., the aorta, tissues, and arteries to assist in healing. Further, the foregoing can be supported by electromagnetic wave or sound wave pulsations to further enhance blood flow improvement.

Although it is an advantage of the device to not need to cross the aortic valve, in certain embodiments, the described encaged pump system may be combined advantageously with a device that does cross the aortic valve (e.g., in high head/low flow applications). Such a system includes placement of the device that does cross the aortic valve at the tip of the catheter, beyond the aortic valve and placement of the herein described second device encaged impeller (bare aortic stent and pump on the catheter) proximal the renal arteries that feed the kidneys. The first such pump may be a second of the herein described pumps or a pump akin to the HeartMate PHP percutaneous heart pump. The second such pump may be that of FIG. 11 adapted by extending the drive shaft further to interact and drive the first pump. The two pumps are placed on the same catheter and may utilize the same drive shaft. The first pump operating high near the heart (for left ventricle unloading) past the heart valve and the second pump in positioned in the lower aorta, just above the renal arteries (for renal output improvement), i.e., the second pump in the mid to lower stomach and the first pump up in the upper mid chest (usually 20 to 30 cm in most people).

In such a situation, sometimes the required operating conditions for a subject are beyond the reach of a single, standard pump, and it is best to combine simple pump performances that add up to the necessary requirements. Positioning pumps in series as described herein, or connected along a single line, allows the system to add the head from each pump together to meet the high head, low flow system requirements. This is because the fluid pressure increases as the continuous flow passes through each pump, much like how a multi-stage pump works. For example, if two of the same pumps are in series, the combined performance curve will have double the head of a single pump for a given flow rate. For two different pumps, the head is still added together on the combined pump curve, but the curve will most likely have a piecewise discontinuity.

In situations where a high, constant pressure is required, speed control may need to be included with, for example, the first pump in such a system. This configuration achieves the high pressure that is needed, while keeping a low flow, because the fixed-speed pump feeds into the speed-controlled pump, which adjusts its output with a pressure transmitter to add only enough head to maintain a constant pressure. This device would combine the benefits of both designs in one product. Having two in series reduces RPMs needed for both to get same flow improvement.

The disclosure is further described with the aid of the following Examples.

EXAMPLE I

The herein described circulatory assist device is combined with a heart regeneration bioelectric stimulator, micro infusion pump, and mixed composition for implantation into a subject's aorta as described herein. In such a combination, the circulatory assist pump off loads work load from the heart, thus improving perfusion to improve regeneration results. The subject's heart recovers over time.

Expression of desirable protein(s) may be accomplished via, e.g., implanted micro coils on the stent. See, e.g., the earlier incorporated US Patent publication US 2017/0266371 A1 to Leonhardt et al. (Sep. 21, 2017) and/or the earlier incorporated Macfelda et al., “Bioelectrical signals improve cardiac function and modify gene expression of extracellular matrix components,” ESC Heart Failure 2017; 4: 291-300 (published online 30 Jun. 2017).

As previously described, such micro coils too can utilize wireless energy. Wireless control extends to pulsatility, speed, and/or impeller angle of the various components of the system.

EXAMPLE II

As depicted in FIG. 11 , a physiologically accurate mock circulation loop (static mock flow loop) is used to test the devices at the Cardiovascular Innovation Institute in Louisville, KY. FIG. 11 shows the dynamic mock flow loop includes (a) a left ventricle, (b) a left ventricular assist device (LVAD), (c) systemic compliance, (d) venous reservoir, and (e) atrial elements. These mock flow loops quantify the hydraulic and hemodynamic performance of the LVAD.

EXAMPLE III

An impeller 10 (FIGS. 1-4 ) is made and encaged within a stent cage 32 (FIG. 15 ) placed near the catheter's tip 34. The impeller blades 14, 16 are 14.5 mm long from tip to tip and are made of 17-4PH stainless steel.

The circulatory assist pump (FIG. 15 ) is placed in the subject's aorta just above the renal arteries. The stent cage is expanded and the impeller blades extended within the aorta.

The impeller blades are set to rotate at 7,500 rpm in a 20 mm aorta distended with stent radial force to 22 mm, thus producing an increase of 1.5 liters per minute flow from a starting base of 3.5 liters per minute increasing to 5.0 liters per minute total flow in the aorta just above the renal arteries. Dependent on, for example, the subject being treated, an optimal pump speed can be as high as 10,000 rpm.

Computational fluid dynamics testing is conducted used to determine flow rates (particularly flow into the renal arteries), aortic pressure differential, and coronary flow rates, and thus brain and hemolysis risk.

EXAMPLE IV

A circulatory assist pump is made and encaged within a stent cage. The impeller blades have an impeller diameter of 13.5 mm long from tip to tip and are made of 17-4PH stainless steel.

The impeller blades are set to rotate at 7,500 rpm in an open stent (outer diameter) aorta distended of 22.86 mm.

The boundary conditions are as follows:

Flow Inlet (L/min) of 3.5, 4.5, and 5.5.

Impeller speeds (rpm) of 7,500, 10,500, and 15,000.

EXAMPLE V

An upper aortic pulsating stent graft useful herein has the following dimensions and specifications:

Outer Diameter of 24 mm aortic stent for being placed, e.g., in a 20-22 mm aorta

Total Length of 6 cm before placement in the 22 mm aorta (lengthens when compressed).

Hoop Strength of 15.8 N/cm

Radial Resistance Force of 1.27 N/cm

Chronic Outward Force of 0.31 N/cm

Three (3) pulsating wireless powered bands each 1.5 cm wide each wrapped around stent. Only one pulsates at any given time.

Aortic stent is three-quarters covered in ePTFE (expanded polytetrafluoroethylene) matching with positions of pulsatile bands.

Each pulse band on each pulsation moves covered stent inward into the aorta 3 mm (a 3 mm aortic pulse wave).

Pulsation is time matched to natural pulses of the subject's heart (e.g., “native flow”) with a slight time delay for time for pulsed blood flow to reach the aorta.

EXAMPLE VI

Powering an impeller pump positioned within a stent cage similar to that of FIG. 16 was successfully demonstrated by the Queensland University of Technology (QUT) in Brisbane, Australia, using the QUT wireless power system. An AC/DC power supply providing 1.6 volts connected to a transmitter coil to a series capacitor coil and inverter (set at 1 megahertz) and controller. The system was about 1.3 Watt.

REFERENCES

The contents of each of the following references are incorporated herein by this reference:

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1. A system for a wireless circulatory assist pump, the system comprising: a wireless circulatory assist pump comprising: a first portion at a first end, the first portion comprising: a battery at a distal end of the first portion; a motor at a proximal end of the first portion; and circuitry interposed between the battery and the motor; and a second portion at a second end opposite the first end; a stent cage between and connected to the first portion and the second portion, the stent cage of a size and shape to allow a highly open flow when placed within a subject's aorta while maintaining pulsatility of the subject's aortic wall; and an impeller encaged by the stent cage and connected to the first portion and the second portion, the impeller comprising blades configured to pump blood through the subject's aorta upon being driven by the motor.
 2. The system of claim 1, wherein the second end of the second portion is configured to removably connect to a catheter.
 3. The system of claim 1, wherein the second portion comprises an annular groove.
 4. The system of claim 1, wherein the first portion has a first mass greater than a second mass of the second portion.
 5. The system of claim 4, wherein a ratio of the second mass to the first mass is within a range of from about 15:1 to about 2:1.
 6. The system of claim 1, wherein the first portion comprises a hermetically sealed canister encompassing the motor, the circuitry, and the battery.
 7. The system of claim 6, wherein the hermetically sealed canister comprises a biocompatible ceramic portion surrounding the circuitry, and a biocompatible polymer portion surrounding the battery and the motor.
 8. The system of claim 1, wherein the circuitry comprises a wireless charging circuit, a communications circuit, and a control circuit.
 9. The system of claim 8, wherein the wireless charging circuit is in electronic communication with the battery and the motor.
 10. The system of claim 1, further comprising a catheter connected to the second end of the wireless circulatory assist pump.
 11. A system for a wireless circulatory assist pump, the system comprising: a deployment catheter comprising: an outer sheath; an inner member within the outer sheath, the inner member configured to move axially relative to the outer sheath such that the deployment catheter transitions between a retracted position and an extended position; and a plurality of fingers positioned radially between the outer sheath and the inner member, a finger of the plurality of fingers biased radially outward such that the finger extends radially outward when the deployment catheter is in the extended position.
 12. The system of claim 11, wherein each of the plurality of fingers are biased radially outward.
 13. The system of claim 11, wherein a tip of each of the plurality of fingers comprises a protrusion.
 14. The system of claim 13, wherein the protrusion at the tip of each of the plurality of fingers is positioned to engage and hold an end of a wireless circulatory assist pump in response to the outer sheath being deployed over the plurality of fingers, and to disengage and release the end of a wireless circulatory assist pump in response to the outer sheath being retracted from over the plurality of fingers.
 15. The system of claim 13, wherein the protrusion of each of the plurality of fingers are magnetic.
 16. The system of claim 11, wherein the plurality of fingers are equidistantly spaced from one another.
 17. A system for a wireless circulatory assist pump, the system comprising: a retrieval catheter, comprising: an outer sheath; an inner member within the outer sheath and configured to move axially relative to the outer sheath such that the retrieval catheter transitions between a retracted position and an extended position, the inner member comprising a magnetic end; and a plurality of fingers positioned radially between the outer sheath and the inner member, a finger of the plurality of fingers biased radially outward such that the finger extends radially outward when the retrieval catheter is in the extended position.
 18. The system of claim 17, wherein the magnetic end of the inner member comprises a spherical magnet secured to an end of the inner member.
 19. The system of claim 17, wherein the magnetic end is configured to be received within a recess at an end of a wireless circulatory assist pump corresponding to the shape and size of the magnetic end.
 20. The system of claim 17, wherein the magnetic end is configured to engage with a ferromagnetic end of a wireless circulatory assist pump. 